Evidence map›Paper›PMID 36132282›Full record

ArticleNanoscale advances2022

Analysis of cell-nanoparticle interactions and imaging of

Michihiro Nakamura, Junna Nakamura, Chihiro Mochizuki, Chika Kuroda, Shigeki Kato, Tomohiro Haruta, Mayu Kakefuda, Shun Sato, Fuyuhiko Tamanoi, Norihiro Sugino

Open access · goldAbstract read
In one paragraph

Article in Nanoscale advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Michihiro NakamuraDepartment of Organ Anatomy and Nanomedicine, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan nakam@yamaguchi-u.ac.jp.ORCID https://orcid.org/0000-0002-9216-3215
Junna NakamuraDepartment of Organ Anatomy and Nanomedicine, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan nakam@yamaguchi-u.ac.jp.
Chihiro MochizukiDepartment of Organ Anatomy and Nanomedicine, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan nakam@yamaguchi-u.ac.jp.
Chika KurodaDepartment of Organ Anatomy and Nanomedicine, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan nakam@yamaguchi-u.ac.jp.
Shigeki KatoDepartment of Organ Anatomy and Nanomedicine, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan nakam@yamaguchi-u.ac.jp.
Tomohiro HarutaEM Application Group, EM Business Unit, JEOL Ltd. Japan.
Mayu KakefudaEM Application Group, EM Business Unit, JEOL Ltd. Japan.
Shun SatoDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan.
Fuyuhiko TamanoiDepartment of Microbiology, Immunology and Molecular Genetics, University of California Los Angeles CA 90095 USA.
Norihiro SuginoDepartment of Obstetrics and Gynecology, Graduate School of Medicine, Yamaguchi University 1-1-1 Minami-Kogushi Ube Yamaguchi 755-8505 Japan.
Yamaguchi University · JPJEOL (Japan) · JPUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomedical imaging using cell labeling is an important technique to visualize cell dynamics in the body. To label cells, thiol-organosilica nanoparticles (thiol-OS) containing fluorescein (thiol-OS/Flu) and rhodamine B (thiol-OS/Rho) were surface-functionalized with polyethyleneimine (PEI) (OS/Flu-PEI and OS/Rho-PEI) with 4 molecular weights (MWs). We hypothesized PEI structures such as brush, bent brush, bent lie-down, and coiled types on the surface depending on MWs based on dynamic light scattering and thermal gravimetric analyses. The labeling efficacy of OS/Flu-PEIs was dependent on the PEI MW and the cell type. A dual-particle administration study using thiol-OS and OS-PEIs revealed differential endosomal sorting of the particles depending on the surface of the NPs. The endosomes in the labeled cells using OS/Flu-PEI and thiol-OS/Rho revealed various patterns of fluorescence termed barcoded endosomes. The cells labeled with OS-PEI

Identifiers

PMID36132282
PMCPMC9417756
OpenAlexW4285186365

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.